Zhang Jingjing, Zhou Rui, Cao Guangzhao, Zhang Yi, Xu He, Yang Hongjun
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Chinese Institute for Brain Research, Beijing, China.
Front Pharmacol. 2022 Mar 21;13:818245. doi: 10.3389/fphar.2022.818245. eCollection 2022.
C5ar1 (CD88) has been identified as an important potential therapeutic target for regulating inflammation in ischemic stroke. In this study, the neuroprotective effect of Guhong injection (GHI) on middle cerebral artery occlusion (MCAO)-induced reperfusion injury was assessed and the mechanism was explored by RNA-seq technology. GHI administered for 6 consecutive days significantly decreased body weight loss, infarction rate, neurological deficient scores, and neuron loss but improved rat survival percentage and regional cerebral blood flow after MCAO surgery. Furthermore, we identified inflammation as a vital process and C5AR1 as a vital target in GHI-mediated protection by using RNA-seq analysis. Further experiments confirmed that GHI decreased C5AR1, C5A, CASP3, 8-OHdG, and inflammatory factors such as IL-1β, TNF, IL6, ICAM-1, MMP9, and MCP-1, and enhanced the expression of TIMP1, JAM-A, and laminin. Furthermore, GHI and its major components hydroxysafflower yellow A (HSYA) and aceglutamide (AG) enhanced cell viability and reduced LDH level and C5AR1 expression in a C5A-induced Neuro-2a cell damage model. In general, this study elucidated the mechanism of GHI against ischemic stroke by inhibiting inflammation and highlighted the potential important role of C5AR1 in ischemic stroke. This research provided new insights into the mechanism of GHI in resisting ischemic stroke and benefits of its clinical application.
C5ar1(CD88)已被确定为调节缺血性中风炎症的重要潜在治疗靶点。在本研究中,评估了骨红注射液(GHI)对大脑中动脉闭塞(MCAO)诱导的再灌注损伤的神经保护作用,并通过RNA测序技术探索其机制。连续6天给予GHI可显著减少体重减轻、梗死率、神经功能缺损评分和神经元损失,但可提高MCAO手术后大鼠的存活率和局部脑血流量。此外,通过RNA测序分析,我们确定炎症是一个关键过程,C5AR1是GHI介导的保护作用中的关键靶点。进一步的实验证实,GHI可降低C5AR1、C5A、CASP3、8-羟基脱氧鸟苷(8-OHdG)以及白细胞介素-1β(IL-1β)、肿瘤坏死因子(TNF)、白细胞介素-6(IL6)、细胞间黏附分子-1(ICAM-1)、基质金属蛋白酶-9(MMP9)和单核细胞趋化蛋白-1(MCP-1)等炎症因子的表达,并增强基质金属蛋白酶组织抑制因子1(TIMP1)、连接黏附分子A(JAM-A)和层粘连蛋白的表达。此外,在C5A诱导的Neuro-2a细胞损伤模型中,GHI及其主要成分羟基红花黄色素A(HSYA)和乙酰谷酰胺(AG)可提高细胞活力,降低乳酸脱氢酶(LDH)水平和C5AR1表达。总体而言,本研究阐明了GHI通过抑制炎症来对抗缺血性中风的机制,并突出了C5AR1在缺血性中风中的潜在重要作用。本研究为GHI抵抗缺血性中风的机制及其临床应用的益处提供了新的见解。